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2. Assignment of the tibial muscular dystrophy locus to chromosome 2q31. Haravuori H; Mäkelä-Bengs P; Udd B; Partanen J; Pulkkinen L; Somer H; Peltonen L Am J Hum Genet; 1998 Mar; 62(3):620-6. PubMed ID: 9497249 [TBL] [Abstract][Full Text] [Related]
3. [Tibial muscular dystrophy. A rare form of distal myopathy]. de Seze J; Udd B; Vermersch P Rev Neurol (Paris); 1999 Apr; 155(4):296-305. PubMed ID: 10367327 [TBL] [Abstract][Full Text] [Related]
4. The first European family with tibial muscular dystrophy outside the Finnish population. de Seze J; Udd B; Haravuori H; Sablonnière B; Maurage CA; Hurtevent JF; Boutry N; Stojkovic T; Schraen S; Petit H; Vermersch P Neurology; 1998 Dec; 51(6):1746-8. PubMed ID: 9855539 [TBL] [Abstract][Full Text] [Related]
5. Tibial muscular dystrophy in a Belgian family. Van den Bergh PY; Bouquiaux O; Verellen C; Marchand S; Richard I; Hackman P; Udd B Ann Neurol; 2003 Aug; 54(2):248-51. PubMed ID: 12891679 [TBL] [Abstract][Full Text] [Related]
6. Tibial muscular dystrophy is a titinopathy caused by mutations in TTN, the gene encoding the giant skeletal-muscle protein titin. Hackman P; Vihola A; Haravuori H; Marchand S; Sarparanta J; De Seze J; Labeit S; Witt C; Peltonen L; Richard I; Udd B Am J Hum Genet; 2002 Sep; 71(3):492-500. PubMed ID: 12145747 [TBL] [Abstract][Full Text] [Related]
14. Clinical and molecular analysis of a large family with three distinct phenotypes of progressive muscular dystrophy. Illarioshkin SN; Ivanova-Smolenskaya IA; Tanaka H; Vereshchagin NV; Markova ED; Poleshchuk VV; Lozhnikova SM; Sukhorukov VS; Limborska SA; Slominsky PA; Bulayeva KB; Tsuji S Brain; 1996 Dec; 119 ( Pt 6)():1895-909. PubMed ID: 9009996 [TBL] [Abstract][Full Text] [Related]
15. Titinopathies and extension of the M-line mutation phenotype beyond distal myopathy and LGMD2J. Udd B; Vihola A; Sarparanta J; Richard I; Hackman P Neurology; 2005 Feb; 64(4):636-42. PubMed ID: 15728284 [TBL] [Abstract][Full Text] [Related]
16. The phenotype of chromosome 2p-linked limb-girdle muscular dystrophy. Mahjneh I; Passos-Bueno MR; Zatz M; Vainzof M; Marconi G; Nashef L; Bashir R; Bushby K Neuromuscul Disord; 1996 Dec; 6(6):483-90. PubMed ID: 9027859 [TBL] [Abstract][Full Text] [Related]
17. Early onset muscular dystrophy with autosomal dominant heredity. Report of a family and CT findings of skeletal muscle. Tohyama J; Inagaki M; Nonaka I Brain Dev; 1994; 16(5):402-6. PubMed ID: 7892962 [TBL] [Abstract][Full Text] [Related]
18. Muscular dystrophy with separate clinical phenotypes in a large family. Udd B; Kääriänen H; Somer H Muscle Nerve; 1991 Nov; 14(11):1050-8. PubMed ID: 1745277 [TBL] [Abstract][Full Text] [Related]
19. Distal muscular dystrophy with autosomal recessive inheritance. Scoppetta C; Vaccario ML; Casali C; Di Trapani G; Mennuni G Muscle Nerve; 1984; 7(6):478-81. PubMed ID: 6543900 [TBL] [Abstract][Full Text] [Related]